A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9803002



Internal ID18330211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23574141..23582626hg38UCSC Ensembl
Innerchr13:24148280..24156765hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg388486
hg198486
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3580574
Supporting Variants
Samples401491BB
Known GenesTNFRSF19
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
CommentsNumber of probes=8
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9803002
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer